or apply directly on Azurity Pharmaceuticals - US's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 81 days Azurity Pharmaceuticals - US's roles stay open a median of 66 days
- Reposted
- No
- Salary listed
- No 0% of Azurity Pharmaceuticals - US's roles list one
- Ghost-job risk at Azurity Pharmaceuticals - US
- high 87 stale, 0 reposted of 87 open
- Hiring momentum
- 114 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-10-23
Measured from postings appearing on and disappearing from Azurity Pharmaceuticals - US's own greenhouse board since 2026-08-03. Full hiring picture for Azurity Pharmaceuticals - US.
About this role
The Senior Clinical Project Manager at Azurity Pharmaceuticals will lead the planning and execution of domestic and global postmarketing clinical trials. This role involves collaborating with various departments and external vendors to ensure trials are completed on time, within budget, and compliant with regulations. Responsibilities include managing study timelines, vendor oversight, and ensuring quality standards are met throughout the clinical development process.
- benefits
- 1/5
- freshness
- 1/5
- career value
- 4/5
- role clarity
- 5/5
- pay transparency
- 0/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Azurity Pharmaceuticals - US as an employer.
What you need
- Bachelor's degree in Life Sciences or a related scientific discipline
- 8+ years of Clinical Trial / Project Management experience within CRO, biotechnology or pharmaceutical organizations
- Demonstrated experience operating at a Senior Clinical Trial Lead or Associate Director level
- Proven leadership of global clinical studies and cross-functional project teams
- Strong experience managing CROs, vendors, and external partners
- Extensive knowledge of ICH-GCP, FDA, EMA, and global clinical trial regulations
Nice to have
- 5+ years’ experience of clinical trial management for late phase studies
- Experience with IMP/clinical drug supply logistics, planning, and labeling activities in late phase studies
- Effective communicator who can manage multiple priorities while building strong internal relationships across multiple departments
Worth weighing
- No salary listed
- Role involves significant cross-functional collaboration and vendor management
- Focus on late phase clinical trials may limit exposure to earlier phases
Summarised from Azurity Pharmaceuticals - US's posting. Read the full original.
Listed by Azurity Pharmaceuticals - US on their greenhouse job board, last confirmed open on 2026-10-23. PitchMeAI is not the employer.
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